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Miconazole Nitrate
Miconazole Nitrate - 0713-0252-37 - (Miconazole Nitrate)
Drug Information of Miconazole Nitrate
| Product NDC: | 0713-0252 |
| Proprietary Name: | Miconazole Nitrate |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | 20 mg/g & nbsp; Miconazole Nitrate |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Miconazole Nitrate
| Product NDC: | 0713-0252 |
| Labeler Name: | G&W Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074366 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960222 |
Package Information of Miconazole Nitrate
| Package NDC: | 0713-0252-37 |
| Package Description: | 45 g in 1 TUBE, WITH APPLICATOR (0713-0252-37) |
NDC Information of Miconazole Nitrate
| NDC Code | 0713-0252-37 |
| Proprietary Name | Miconazole Nitrate |
| Package Description | 45 g in 1 TUBE, WITH APPLICATOR (0713-0252-37) |
| Product NDC | 0713-0252 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | VAGINAL |
| Start Marketing Date | 19960222 |
| Marketing Category Name | ANDA |
| Labeler Name | G&W Laboratories, Inc. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
